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08 August 2012

Description Of Good Clinical Practices

By Shari Swanson


Whenever a company, university or group of scientists is conducting research that involves other people, they need to follow a set of strict rules known as good clinical practices. These rules ensure that people who are being studied are protected and not harmed. This article aims to give more knowledge on the concept of these rules and how to follow them when conducting research.

Before any new medicine or medical procedure can start to be used by the public, there must be extensive research conducted on people to make sure that the drug or procedure is safe. There is always a risk of harm to people who are involved in a trial, so these trials have to be completed in a way that is ethical and as safe as possible.

Sometimes investigators may also be at risk of exploiting the trial participants, as they have less knowledge about the medical field. To prevent this, guidelines were developed that have to be followed by anyone who is conducting a trial involving people, anywhere in the world.

These guidelines aim to protect the rights of people involved in studies. They also help the study results to be more accurate, which means they can be better used to help other people in the future, and the results of using the new medication can be predicted.

The guidelines attempt to create a standard that has to be followed by countries across the world. There are a number of principles that have to be adhered to in order to meet the requirements for the guidelines. For example, a trial should only be conducted if the benefits of the trial outweigh the risks, and investigators have to keep in mind that the safety of the people enrolled in the trial is more important than any contribution to science or society.

Anyone who conducts research on human beings needs to follow good clinical practices it is an ethical requirement and the only way to make sure the study results will be accepted across the world.




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